Fructose Intolerance Genetic Test Kit

A molecular diagnostics reagent kit for human MTHFR gene typing using PCR with fluorescent probes. The kit enables genetic analysis for clinical and personalized medicine applications.

A molecular detection kit for identifying hereditary disease markers and genetic predispositions. Designed for clinical screening and diagnostic purposes in genetic medicine applications.

PCR-CE FMR1 kit is a molecular diagnostic test for detecting FMR1 gene mutations associated with Fragile X Syndrome. The kit enables rapid and accurate identification of carrier status and disease presence, supporting genetic screening and diagnosis in maternal and pediatric healthcare settings.

Molecular diagnostic kit for genetic testing and variant detection. Supports precision medicine applications in cardiovascular and oncology disease management.

Specialized PCR diagnostic kit for detection of rare genetic diseases. Targets uncommon genetic mutations and chromosomal abnormalities.

A gene genotyping detection kit for human MTHFR gene analysis using PCR with fluorescent probe methodology. It enables genetic testing for personalized medicine applications. Available variants: Human MTHFR Gene Genotyping Detection Kit (PCR Fluorescent Probe Method).

Diagnostic test kit for identification of genetic mutations and inherited disorders through nucleic acid sequencing. Supports clinical genetic testing and carrier screening applications.

PCR-based detection kit for identifying cystic fibrosis transmembrane conductance regulator mutations in patient samples. Enables genetic screening for cystic fibrosis susceptibility and diagnosis.

A diagnostic solution for identifying lactose intolerance through laboratory analysis. The system provides reliable assessment of patient tolerance to lactose consumption.

Diagnostic kit using PCR methodology for identifying genetic mutations and polymorphisms. Supports clinical diagnosis of genetic disorders and carrier screening.

PCR-based fluorescence hybridization kit for genetic deafness gene detection and screening. Identifies hereditary hearing loss mutations through real-time PCR flow cytometry analysis, enabling early diagnosis and genetic counseling in clinical and research laboratories.

A diagnostic test kit for detecting the MTHFR A1298C mutation associated with genetic predisposition to thrombophilia. The kit contains reagents for 32 tests and is compatible with QiaSymphony SP/AS extraction systems. It is CE Mark certified.